Atlas FDA

TECHNICON H*1 SYSTEM

FDA 510(k) clearance K852787 · decided 1985-07-23

Clearance details

K-number
K852787
Device name
TECHNICON H*1 SYSTEM
Applicant
Technicon Instruments Corp.
Decision
Substantially Equivalent
Date received
1985-07-01
Decision date
1985-07-23
Days to decision
22 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Tarrytown, NY, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.